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(R)-(-)-1-(4-氟苯氧基)-2-丙醇 | 307532-03-2

中文名称
(R)-(-)-1-(4-氟苯氧基)-2-丙醇
中文别名
(R)-(-)-1-(4-氟丙氧基)-2-丙醇
英文名称
(2R)-1-(4-fluorophenoxy)propan-2-ol
英文别名
(R)-(-)-1-(4-Fluorophenoxy)-2-propanol
(R)-(-)-1-(4-氟苯氧基)-2-丙醇化学式
CAS
307532-03-2
化学式
C9H11FO2
mdl
——
分子量
170.184
InChiKey
RIFIEDWKCIVRQN-SSDOTTSWSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    47-51 °C (lit.)
  • 闪点:
    >230 °F
  • 稳定性/保质期:
    常温常压下稳定,避免与强氧化物、强酸和强碱接触。

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2909499000
  • WGK Germany:
    3

反应信息

  • 作为反应物:
    描述:
    (R)-(-)-1-(4-氟苯氧基)-2-丙醇三乙胺N,N-二异丙基乙胺 作用下, 以 二氯甲烷二甲基亚砜 为溶剂, 反应 482.08h, 生成 1'-[(1S)-2-(4-fluorophenoxy)-1-methylethyl]-6-methoxy-2,3,4,9-tetrahydrospiro[β-carboline-1,3'-pyrrolidine] trifluoroacetate
    参考文献:
    名称:
    [EN] TETRAHYDROSPIRO-BETA-CARBOLINE-1,3 '-PYRROLIDINE DERIVATIVES AND THEIR USE IN GHSR-RELATED DISORDERS
    [FR] NOUVELLES CARBOLINES-BETA EN TANT QU'ANTAGONISTES DE RECEPTEUR DE SECRETAGOGUE D'HORMONE DE CROISSANCE
    摘要:
    公开号:
    WO2005048916A3
点击查看最新优质反应信息

文献信息

  • 4,5-DIHYDRO-OXAZOL-2YL DERIVATIVES
    申请人:Galley Guido
    公开号:US20100029589A1
    公开(公告)日:2010-02-04
    The invention relates to compounds of formula I wherein R 1 , R 2 , X, Y, and n are defined in the specification and to pharmaceutically acceptable acid addition salts thereof. The invention also provides pharmaceutical compositions and methods of manufacture of such compounds. The compounds are useful for the treatment of diseases related to the biological function of the trace amine associated receptors, which diseases are depression, anxiety disorders, bipolar disorder, attention deficit hyperactivity disorder, stress-related disorders, psychotic disorders, schizophrenia, neurological diseases, Parkinson's disease, neurodegenerative disorders, Alzheimer's disease, epilepsy, migraine, substance abuse and metabolic disorders, eating disorders, diabetes, diabetic complications, obesity, dyslipidemia, disorders of energy consumption and assimilation, disorders and malfunction of body temperature homeostasis, disorders of sleep and circadian rhythm, and cardiovascular disorders.
    该发明涉及公式I的化合物,其中R1、R2、X、Y和n在规范中定义,并且其药学上可接受的酸盐。该发明还提供了制备这种化合物的药物组合物和方法。这些化合物可用于治疗与痕量胺相关受体的生物功能相关的疾病,这些疾病包括抑郁症、焦虑症、躁郁症、注意缺陷多动障碍、与压力有关的疾病、精神疾病、精神分裂症、神经系统疾病、帕金森病、神经退行性疾病、阿尔茨海默病、癫痫、偏头痛、物质滥用和代谢紊乱、进食障碍、糖尿病、糖尿病并发症、肥胖症、脂质代谢异常、能量消耗和吸收异常、体温稳态异常、睡眠和昼夜节律异常、心血管疾病。
  • [EN] LEVODOPA PRODRUGS, AND COMPOSITIONS AND USES THEREOF<br/>[FR] PROMEDICAMENTS DE LEVODOPA, ET COMPOSITIONS ET LEURS UTILISATIONS
    申请人:XENOPORT INC
    公开号:WO2005121070A1
    公开(公告)日:2005-12-22
    Prodrugs of levodopa, methods of making prodrugs of levodopa, methods of using prodrugs of levodopa, and compositions of prodrugs of levodopa are disclosed. Formula (I), n is an integer from 1 to 6; R5 is selected from alkyl, substituted alkyl, aryl, substituted aryl, arylalkyl, substituted arylalkyl, cycloalkyl, substituted cycloalkyl, heteroalkyl, substituted heteroalkyl, cycloheteroalkyl, substituted cycloheteroalkyl, heteroalyl, substituted heteroalyl, heteroalylalkyl, and substituted heteroalylalkyl.
    本文披露了左旋多巴的前药、制备左旋多巴前药的方法、使用左旋多巴前药的方法以及左旋多巴前药的组合物。其中,公式(I)中,n为1至6的整数;R5选自烷基、取代烷基、芳基、取代芳基、芳基烷基、取代芳基烷基、环烷基、取代环烷基、杂烷基、取代杂烷基、环杂烷基、取代环杂烷基、杂烯基、取代杂烯基、杂烯基烷基和取代杂烯基烷基。
  • Beta-carbolines as growth hormone secretagogue receptor (GHSR) antagonists
    申请人:Crossley Roger
    公开号:US20050288316A1
    公开(公告)日:2005-12-29
    The present invention relates to compounds of Formula (I): wherein R 3 -R 8 , X, and Y are as described herein, processes for preparing the compounds, pharmaceutical compositions comprising the compounds, and use of the compounds and compositions in the prophylaxis or treatment of a GHSR receptor-related disorder. Examples of such disorders are obesity and related disorders such as diabetes type II, dyslipidemia and the metabolic syndrome Prader-Willi syndrome, cardiovascular diseases such as atherosclerotic vascular disease, angina pectoris, myocardial infarction and stroke, acromegaly and cancer, in particular breast, lung, prostate, thyroid and endocrine pituary carcinomas.
    本发明涉及式(I)的化合物:其中R3-R8,X和Y如本文所述,制备该化合物的方法,包含该化合物的药物组合物,以及在预防或治疗与GHSR受体相关的疾病中使用该化合物和组合物。此类疾病的例子包括肥胖症和相关疾病,如2型糖尿病,血脂异常和代谢综合征,普拉德-威利综合征,心血管疾病,如动脉粥样硬化、心绞痛、心肌梗死和中风,肢端肥大症和癌症,特别是乳腺癌、肺癌、前列腺癌、甲状腺癌和内分泌腺垂体癌。
  • Levodopa prodrugs, and compositions and uses thereof
    申请人:Xiang Jia-Ning
    公开号:US20060020028A1
    公开(公告)日:2006-01-26
    Prodrugs of levodopa, methods of making prodrugs of levodopa, methods of using prodrugs of levodopa, and compositions of prodrugs of levodopa are disclosed.
    本研究公开了左旋多巴原药、左旋多巴原药的制作方法、左旋多巴原药的使用方法以及左旋多巴原药的组合物。
  • 4,5-DIHYDRO-OXAZOL-2-YL DERIVATIVES
    申请人:F. Hoffmann-La Roche AG
    公开号:EP2321287A1
    公开(公告)日:2011-05-18
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